Development of the Static and Dynamic Gene Expression Regulation Toolkit in Pseudomonas chlororaphis.
ACS Synth Biol
; 13(3): 913-920, 2024 03 15.
Article
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| MEDLINE
| ID: mdl-38377538
ABSTRACT
The advancement of metabolic engineering and synthetic biology has promoted in-depth research on the nonmodel microbial metabolism, and the potential of nonmodel organisms in industrial biotechnology is becoming increasingly evident. The nonmodel organism Pseudomonas chlororaphis is a safe plant growth promoting bacterium for the production of phenazine compounds; however, its application is seriously hindered due to the lack of an effective gene expression precise regulation toolkit. In this study, we constructed a library of 108 promoter-5'-UTR (PUTR) and characterized them through fluorescent protein detection. Then, 6 PUTRs with stable low, intermediate, and high intensities were further characterized by report genes lacZ encoding ß-galactosidase from Escherichia coli K12 and phzO encoding PCA monooxygenase from P. chlororaphis GP72 and thus developed as a static gene expression regulation system. Furthermore, the stable and high-intensity expressed PMOK_RS0128085UTR was fused with the LacO operator to construct an IPTG-induced plasmid, and a self-induced plasmid was constructed employing the high-intensity PMOK_RS0116635UTR regulated by cell density, resulting in a dynamic gene expression regulation system. In summary, this study established two sets of static and dynamic regulatory systems for P. chlororaphis, providing an effective toolkit for fine-tuning gene expression and reprograming the metabolism flux.
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1
Bases de datos:
MEDLINE
Asunto principal:
Pseudomonas chlororaphis
Idioma:
En
Revista:
ACS Synth Biol
/
ACS synth. biol
/
ACS synthetic biology
Año:
2024
Tipo del documento:
Article
País de afiliación:
China